Sealing glass composite
The present direct invention is directed to a sealing glass composite comprising a low melting point sealing glass matrix mixed with a particulate additive to increase the effective coefficient of thermal expansion of the resulting sealing glass composite. The sealing glass matrix is in the lead borate family and the particulate additive is preferably calcium fluoride. For extreme bonding conditions, a small amount of copper oxide is dissolved into the glass matrix.
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The invention and further developments of the invention are now elucidated by means of the preferred embodiments in the drawings.
FIG. 1 is a cross-sectional view of a prior art ceramic dual-in-line package;
FIG. 2 is a cross-sectional view through a metal quad-in-line package incorporating the sealing glass composite of the present invention; and
FIG. 3 is a cross-sectional view of a test package in accordance with the present invention.
The present invention sets forth a unique sealing glass composite wherein the matrix comprises a low melting point sealing glass selected from the group consisting of lead borate, lead-zinc borate, lead borosilicate or lead-zinc borosilicate glasses. An additive of a particulate filler which is insoluble or only slightly soluble in the sealing glass matrix is added to increase the effective coefficient of thermal expansion of the resulting glass composite.
The glass matrix of the sealing glass composite of the invention is preferably a complex lead borate type glass matrix generally also containing one or more other glass components, such as bismuth, zinc, aluminum, silicon, barium, arsenic, tin, and tellurium which are normally present in their respective oxide forms. These lead borate type solder glasses usually have a coefficient of thermal expansion of about 80.times.10.sup.-7 to about 130.times.10.sup.-7 in/in/.degree. C. over the temperature range from ambient to their glass transition temperatures (typically about 300.degree. C.).
Such glasses are used in forming vitreous seals and glass-ceramic or semicrystalline seals as known in the electronic packaging art. Weight percent compositional ranges are set forth below in Table I where the total content of all oxides is 100 percent.
TABLE I
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Broad Range
Preferred Range
Oxide (wt. %) (wt. %)
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PbO 70-85 75-85
ZnO 0-20 0.5-16
B.sub.2 O.sub.3
5-15 8-15
SiO.sub.2 0-10 0-5
BaO 0-3 0-2
SnO.sub.2 0-5 0-2
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Other conventional glassmaking oxides such as CaO, Bi.sub.2 O.sub.3, Na.sub.2 O, K.sub.2 O, Li.sub.2 O, CdO, and Fe.sub.2 O.sub.3 can be included. However, it is preferred in many instances not to employ these ingredients but rather to constitute the glass matrix of essentially only those ingredients set forth in Table I above.
In accordance with the present invention, the particulate additive having a high coefficient of thermal expansion as compared with the glass matrix, is preferably calcium flouride or barium fluoride. These materials have limited solubility in the sealing glass at the temperature and times in accordance with this invention. The additive comprises particles having a size between about 1 to about 150 microns. Preferably, the particles have a size between about 10 to about 75 microns. The particle size is limited because smaller particles more readily dissolve in the glass during the sealing process and the sealing glass composite loses the benefit of the high coefficient of thermal expansion of the additive. Conversely, if the particles are too large, the glass flow between them is restrained and their exposed surfaces are prevented from being wet. The result is a loss of strength due to the formation of voids between the interfaces of the particles. The filler or additive has a maximum critical volume content of an effective amount up to about 30 wt. % (60 vol. %) of the glass matrix to prevent particle interlock. Preferably, the filler in the glass matrix is between about 10 to about 20 wt.% (40 to about 60 vol.%) for application to a copper or copper alloy substrate. The filler in the glass matrix has a coefficient of thermal expansion (CTE) which is higher than the CTE of the glass. More importantly, the CTE of the filler must be higher than that of the metal substrate to which it is bonded in order that the CTE of the glass composite can approximate that of the substrate.
The calcium fluoride filler may be supplied as either a man-made, synthetic powder or as fluorspar, the naturally occuring mineral version of the compound. The filler is mixed with powdered sealing glass sized to pass through about 200 mesh or less and preferably through about 400 mesh or less. The sealing glass typically is used to seal packages at a temperature between about 400.degree. C. to about 450.degree. C. The calcium fluoride additive remains inert but wettable at those temperatures. It is a critical aspect of the present invention that the filler is substantially insoluble in the glass matrix at the operative times and temperatures associated with the invention so that the particles remain intact and are not dissolved into the glass. Although it is desirable for a minimum amount of filler to dissolve in the matrix, it is within the scope of the present invention for a maximum of less than about 10 wt. % of the particulate additive to dissolve into the glass. The limited solubility requirement is because the observed increase in thermal expansion arises from a physical mixture of glass and filler, not a modification of the basic glass chemistry.
Fluorspar has a CTE in excess of about 220.times.10.sup.-7 in/in/.degree.C. By contrast, the CTE of materials generally used in electronic packaging is significantly lower as indicated in Table II hereinbelow.
TABLE II
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LINEAR COEFFICIENT OF THERMAL EXPANSION
(CTE) FOR A VARIETY OF MATERIALS USED IN
ELECTRONIC PACKAGING
CTE (.times. 10.sup.-7
MATERIAL in/in/.degree.C.)
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Copper (Cu) 173
Cu Alloy C19500 169
Copper, annealed 168
Cu Alloy C19400 163
Cu Alloy C63800 171
*Sealing Glasses 50-90
Alumina thick film substrate
65
Leadless chip carrier
65
Alumina cofired substrate
64
99.55 BeO 64
Copper clad Invar 64
Thick Film Substrate
64
*96% Alumina 64
*94% Alumina 64
*Kovar 62
*Alloy 42 58
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*used in CERDIP fabrication
Table III lists measured values of CTE for two glasses (PP-200 from Owens Illinois Corp. of Toldeo, Ohio and T-176 from Asahi Corp. of Japan) as a function of CaF.sub.2 loading. The glass composite preferably has a CTE of above about 138.times.10.sup.-7 in/in/.degree. C. (from ambient to glass transition temperature). Table IV below lists the estimated glass composition by weight percent of these glasses. These samples were prepared from a physical mixture of the glass powder and CaF.sub.2 powder which was then heated to a temperature typical of CERDIP sealing (about 430.degree. C. for about 10 minutes). Under these conditions, there is sufficient glass flow to allow complete wetting of the CaF.sub.2 particles, without significant dissolution of the CaF.sub.2 into the glass. The glass characteristically achieves the critical requirement that the filler particles remain intact and are not substantially dissolved into the glass.
TABLE III
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THERMAL EXPANSION MEASUREMENTS
FOR GLASS-FILLER MIXTURES
Expansivity (.times. 10.sup.-7
Glass in/in/.degree.C.) 20-300.degree. C.
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PP-200* 117
PP-200/15% WT. Fluorspar
151
PP-200/20% WT. Fluorspar
158
Asahi T-176** 115
T-176/10% WT. Fluorspar
138
T-176/15% WT. Fluorspar
147
T-176/20% WT. Fluorspar
156
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*Proprietary glass from the Owens Illinois Corp. of Toledo, Ohio.
**Proprietary glass from the Asahi Glass Corp. of Japan.
TABLE IV
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ESTIMATED GLASS COMPOSITIONS BY
WEIGHT PERCENT
PbO B.sub.2 O.sub.3
ZnO SiO.sub.2
SnO.sub.2
Bi.sub.2 O.sub.3
BaO
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T-176* 83.2 11.7 4.1 .55 .3
PP-200**
82.8 11.7 1.0 .5 3.5 .5
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*Proprietary glass from the Asahi Corp.
**Proprietary glass from the Owens Illinois Corp.
To demonstrate the advantage of thermally matched materials, samples of glass to metal seals were produced and tested for torque strength. The samples were fabricated from two 1/4".times.3/4" flat substrates of Cu alloy (either C63800 or a Cu-Ni-Al alloy (B-27) that were sealed together with a glass (Asahi T-176) layer. The various formulations of the glass composite used in conjunction with these tests as well as others described below are set out in Table V.
TABLE V
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GLASS FORMULATIONS
Additions
Sample Glass CaF.sub.2 (wt. %)
CuO (wt. %)
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A T-176* 0 0
B T-176* 15 0
C T-176* 20 0
D T-176* 0 1.4
E T-176* 15 1.4
F T-176* 15 2
G T-176* 20 1.4
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*Proprietary glass from the Asahi Corp.
Data supporting the advantage of matching the coefficients of thermal expansion between the glass composite and the metal substrates by increasing the CTE of the glass composite by additives such as CaF.sub.2 is illustrated in Table VI. Without the CaF.sub.2 addition, stable mechanical bonding was not achieved. In the test samples of metal substrates being sealed together by T-176 without any additions, the glass cracked upon cooling from the initial sealing temperature of about 430.degree. C. By adding 20 wt. % fluorspar to the T-176 glass, stable bonds between the metal substrates and the resulting glass composite were formed as indicated by torque strengths in the range of about 20 to about 40 in. lb. The glass samples correspond to those identified in Table V.
TABLE VI
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TORQUE STRENGTH OF METAL SUBSTRATE-GLASS
COMPOSITE-METAL SUBSTRATE
(using the Asahi T-176 glass)
Torque Strength
(in. lb.)
Metal Substrate
Glass Sample
range Avg.
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Alloy C63800 A 0 0
Alloy C63800 C 20-30 27
Cu--Ni--Al alloy (B-27)
A 0 0
Cu--Ni--Al alloy (B-27)
C 35-40 37
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The importance of limiting particle dissolution is demonstrated by comparing results for PbF.sub.2 and CaF.sub.2 particles added to lead borate type glass. Test data indicate that for the times and temperatures of interest in electronic package sealing (i.e. about 400.degree. C. to about 450.degree. C. for about 5 to about 20 minutes), the presence of up to 20 wt. % (approximately 40 volume %) CaF.sub.2 does not adversely effect the important physical properties of the sealing glasses (i.e. devitrification tendency, flow, chemical resistance, etc.). However, even small amounts of PbF.sub.2 (i.e. <5 volume %), which is soluble in these glasses, can produce enough of an overall chemistry change to initiate rapid devitrification of the glass during a simulated sealing cycle. After devitrification, the glass exhibits a drastic reduction in flow characteristics, and as such would not allow the typical two step sealing operation for CERDIP assembly (i.e. embedding the lead frame into a glass layer covering the surface of the base member; followed by glass sealing the cover onto the lead frame).
Therefore, it is an important aspect of the present invention for the high expansivity, particulate additive to have limited solubility in the glass matrix for the time and/or temperature levels typical of the intended sealing cycles. The particulate is preferably added to the glass when the latter is in powder form. The glass is then melted at a selected temperature whereby the particulate remains intact and does not substantially dissolve into the glass. For example, the glass may be melted, cast or water quenched and milled to powder prior to the CaF.sub.2 addition. The resulting composite of the CaF.sub.2 particulate in a lead borate type glass matrix is distinguished from the prior art glasses such as disclosed in U.S. Pat. No. 4,186,023 to Dumesnil in which fluorides are incorporated directly into the glass during the initial melting, and therefore, are not available as the high expansion second phase required to modify the overall CTE of the resulting glass composite.
BaF.sub.2 is thought to be effective over approximately the same range of about 20 to about 30 wt.% BaF.sub.2 by the glass.
Efforts to use higher thermal conductivity materials for semiconductor casings also require a suitable metal or alloy substrate to enhance the formation of a thermally and mechanically stable glass to metal sealing combination. It is understood that the metals selected for these packages preferably consist of a high thermal conductivity metal or metal alloy such as for example copper or aluminum metals or alloys. The preferred metal or metal alloy of the present invention is a copper or copper base alloy capable of forming a thin refractory oxide layer on at least the surface which is bonded to the glass. An exemplary alloy contains an effective amount of up to about 12% aluminum capable of forming a refractory oxide layer and the balance copper. Preferably, the exemplary alloy consists essentially of from about 1 to 10% aluminum, 0.001 to 3% silicon and optionally, a grain refining element selected from the group consisting of iron up to 4.5%, chromium up to 1%, zirconium up to 0.5%, cobalt up to 1% and mixtures of these grain refining elements and the balance copper. In particular, CDA alloy C63800, as disclosed in U.S. Pat. No. 3,676,292 to Pryor et al., has been demonstrated as suitable. Impurities may be present in the alloy which do not significantly degrade the properties of the alloy or prevent bonding in a desired embodiment. Alloy C63800 has a CTE of about 170.times.10.sup.-7 in/in/.degree. C.
The present invention is not restricted to applications of alloy C63800 but includes the broad field of metals or alloys which have a CTE between about 110 to about 220.times.10.sup.-7 in/in/.degree.C. Preferably, the CTE would be between about 140 to about 180.times.10.sup.-7 in/in/.degree.C. A copper-nickel-aluminum alloy (called B-27 herein) which has been demonstrated to be suitable is disclosed in U.S. Pat. No. 4,434,016 to Saleh et al. The alloy consists essentially of from about 10% to about 15% nickel, from about 1% to about 3% aluminum, up to about 1% manganese, from about 0.05% to less than about 0.5% magnesium and the balance copper. Silicon should not exceed about 0.05%, lead should be less than about 0.015% and phosphorous should be less than about 0.005%. B-27 has a CTE of about 170.times.10.sup.-7 in/in/.degree.C. Other examples of suitable metal alloys, such as nickel base and iron base alloys, are disclosed in U.S. Pat. Nos. 3,698,964, 3,730,779 and 3,810,754.
Metals of the above described composition range have been found to form a satisfactory glass seal with a lead borate type glass sealing composite of the type described hereinabove. The glass composite is preferably a mixture of a low melting point, lead borate type glass matrix and a substantially insoluble, high thermal expansion additive such as calcium fluoride or barium fluoride. The need for the additive has been demonstrated with the data of Table VI. A lead borate type glass lacking a filler (Example A of Table V) which is sealed between metal substrates of either C63800 or B-27 does not form a seal which can sustain any significant torque. However, a lead borate type glass composite including an additive such as CaF.sub.2 (Example C of Table V) which is sealed between metal substrates of either C63800 or B-27 does form a seal which can withstand a significant torque before seal failure.
When the packages of FIGS. 2 and 3 are subjected to extremely adverse conditions such as thermal shock, even the addition of CaF.sub.2 to the glass was not ideal with respect to providing a strong bond between the glass composite and the metal substrates which could withstand the hermeticity and mechanical integrity testing described hereinbelow.
The present invention addresses to the need for an improved glass composite which can withstand extreme operating conditions by further modification of lead borate type glass composite described above with low levels of copper oxide (Cu0). This was demonstrated with glass sample E of Table V where 2 wt. % CuCO3 (the equivalent of 1.4 wt. % Cu0) was added to the Asahi T-176 glass and the modified composition was remelted according to conventional practice. After remelting, the glass was water quenched, dryed, ball milled, and seived to a particle size of about 200 mesh or less. Then the glass was physically mixed with about 15 wt. % fluorspar powder (CaF.sub.2) also having a particle size of about 200 mesh or less.
Testing of the seal between the copper oxide modified glass composite and the metal alloys described above was performed on both Dual-In-Line Packages of the type shown in FIG. 2 and on single sandwich type packages of the type illustrated in FIG. 3. The test package 30, of FIG. 2, includes a metal base member 32. A metal housing member 34 shaped to provide a hollow enclosure for receiving an electronic component 36 is mounted upon the base member. A metal alloy lead frame 38 is glass sealed between the base member and the housing member. The lead frame is connected by wires 40 to an electronic chip component 36 prior to the final sealing of the package. The lead frame 38 has terminal leads 42 and 44 projecting between the base and the housing member external to the casing 30. The terminal leads are sealed and bonded between the base member and the housing member to hermetically seal the casing. The sandwich package 50 of FIG. 3 includes two metal substrate components 52 and 54 bonded together by a sealing glass 56 in accordance with the present invention. The sealing glass for these two types of packages was a lead borate type sealing glass of varied formulation within the ranges specified hereinabove.
Evaluation of the package samples was based on two criteria: (1) hermeticity and (2) mechanical integrity. Hermeticity was measured according to Mil Spec 883B using a helium leak detector. The acceptable standard for this test required each sample to have a helium leak rate below 5.times.10.sup.-8 cm.sup.3 /sec. The acceptable leak rate should be maintained both before and after thermal shock (T.S.) testing (10 cycles, liquid to liquid, -65.degree. C. to +150.degree. C.) These tests were conducted on both sample configurations 30 and 50. (See Table VII and VIII) The mechanical integrity of the sealed package 30 was assessed by the ability of the package to sustain at least 3 cycles of a 90.degree. lead bend without mechanical damage. The choice of 3 bends is arbitrary and not based on a known standard.
In Table VII below, the hermeticity test results of metal packages sealed with glass samples D, E, and G of Table V is set forth. The testing was performed on Dual-In-Line packages as shown in FIG. 2. The base and lid of these packages were fabricated from B-27 and the lead frame from C63800. As might be expected from the test data of Table VI, an alloy base and lid sealed with a glass seal using a lead borate type glass modified with CuO but without a glass filler (sample D), fails to stand up to the hermeticity testing because of the CTE mismatch between the glass and the alloy substrates. The packages cracked while cooling from the sealing temperature of 430.degree. C. When the sample E glass (including both CaF.sub.2 and CuO) was used to seal a Dual-in-Line package, of the type shown in FIG. 2, hermeticity was maintained both before and after exposure to thermal shock. Finally, sample G was used to seal Dual-in-Line packages. The test results indicate that the 20 wt. % fluorspar addition had reached a level where the hermeticity was poor. In actual practice, the amount of fluorspar addition relates to the specific glass composition. For example, if the glass is more vitreous, an effective sealing composition may be composed of a greater percentage of fluorspar than if the glass is less vitreous. Acordingly, the maximum CaF.sub.2 addition is determined in accordance with the specific glass composition to which it is added.
TABLE VII
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HERMETICITY TESTING WITH THE 1.4 WT. % CuO
MODIFIED ASAHI T-176 GLASS SEALING A
DUAL-IN-LINE PACKAGE OF FIG. 2
Hermeticity
Glass Sample Before T.S.
After T.S.
______________________________________
D 0% pass --
(cracked on
cooling)
E 100% pass 100% pass
G 20% pass 0% pass
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In Table VIII below, the test results of the sandwich type package illustrated in FIG. 3 are set forth. The metal substrates were fabricated from C63800 and B-27 and sealed together with the lead borate type glass composite of sample F (Asahi T-176 and having 15 wt. % fluorspar filler) modified by 2 wt. % copper oxide. The test data indicates that this glass did not provide a strong enough bond to the metal substrates to withstand thermal shock.
TABLE VIII
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HERMETICITY TESTING ON SANDWICH SAMPLES
USING SAMPLE F (T-176* WITH 2.0 WT. % CuO
AND 15 WT. % FLUORSPAR FILLER)
Hermeticity
Metal Samples Before T.S.
After T.S.
______________________________________
C63800 5 100% pass fail
B-27 5 100% pass fail
______________________________________
*Proprietary glass of the Asahi Co.
Taking the data of Tables VII and VIII together, the desirability of copper oxide (CuO) addition to the glass has been established as being an effective amount of up to about 2 wt. % for forming a strong enough glass to metal bond having improved capability for withstanding thermal shock. Preferably, the CuO addition to the glass is within the range of about 0.1 to about 2 wt. %.
As set forth in Table IX below, an additional test was performed on a package of the type illustrated in FIG. 1 wherein the cover 34 and the base 32 are fabricated from C63800 while the lead frame 38 is fabricated from B-27. When the sample B glass (T-176 having 15 wt. % fluorspar but no copper oxide) was used to seal the package, a failure between the glass and the metal interface occured before the completion of one bend. However, when the same glass and flourspar filler was modified by providing a copper oxide level of about 1.4 wt. %, the mechanical damage of the seal occured at both the glass-metal interface and within the glass itself after more than three cycles of a 90.degree. lead bend.
TABLE IX
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MECHANICAL INTEGRITY TEST FOR PACKAGE FAB-
RICATED FROM A C63800 LID AND BASE, A B-27 LEAD
FRAME AND SEALED WITH GLASS SAMPLES B AND E
Glass Sample # of bend type of failure
______________________________________
B <1 interfacial
E >3 mixed
______________________________________
The patents, patent applications and publication set forth in this application are intended to be incorporated by reference herein.
It is apparent that there has been provided in accordance with this invention a sealing glass composite which satisfies the objects, means, and advantages set forth hereinabove. While the invention has been described in combination with the embodiments thereof, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alternatives, modifications, and variations as fall within the spirit and broad scope of the appended claims.
Claims
1. A laminate, comprising:
- a substrate consisting of metal or metal alloy;
- a glass composite bonded onto at least a portion of a first surface of said substrate, said glass composite comprising:
- a first component consisting essentially of a vitreous glass matrix selected from the group consisting of lead borate, lead-zinc borate, lead borosilicate and lead-zinc borosilicate glasses, said vitreous glass matrix having a coefficient of thermal expansion in excess of about 80.times.10.sup.-7 in./in./.degree.C. (from ambient to glass transition temperature);
- an effective amount of up to about 2 wt. % of copper oxide being dissolved into said vitreous glass matrix for forming a strong glass to metal bond having improved capability for withstanding thermal shock; and
- a second component mixed into said first component to increase the effective coefficient of thermal expansion of the resulting glass composite to be close to that of said substrate, said second component consisting essentially of an effective amount up to about 30 wt. % of an uncoated particulate additive having limited solubility in said vitreous glass matrix, said uncoated particulate additive having a higher coefficient of thermal expansion that that of said vitreous glass matrix, said uncoated particulate additive having a melting point higher than that of said vitreous glass matrix.
2. The laminate of claim 1 further including a second substrate consisting of metal or metal alloy, said second substrate being bonded to at least a portion of said first substrate by said glass composite.
3. The multilayer laminate of claim 2 in which said second substrate is substantially parallel to said first substrate, and said glass composite is disposed between said first and second substrates.
4. The laminate of claim 1 wherein said uncoated particulate additive is present in said glass composite in an amount from about 10 to about 30 wt. %.
5. The laminate of claim 4 including said uncoated particulate additive being substantially insoluble in said vitreous glass matrix.
6. The laminate of claim wherein less than about 10 wt. % of the uncoated particulate additive mixed in said glass matrix is soluble in said vitreous glass matrix.
7. The laminate of claim 6 wherein said glass composite has a coefficient of thermal expansion of above about 138.times.10.sup.-7 in./in./.degree.C. (from ambient to glass transition temperature).
8. The laminate of claim 7 wherein said vitreous glass matrix consists essentially of by weight about 70 to about 85% PbO, up to about 20% ZnO, between about 5 to about 15% B.sub.2 O.sub.3, up to about 10% SiO.sub.2, up to about 3% BaO and up to about 5% SnO.sub.2.
9. The laminate of claim 7 wherein said glass composite is a sealing glass.
10. The laminate of claim 1 wherein said uncoated particulate is sized from about 10 to about 150 microns.
11. The laminate of claim 10 wherein said uncoated particulate is sized from about 40 to about 150 microns.
12. The laminate of claim 11 wherein said glass composite has a sealing temperature above 400.degree. C.
13. The laminate of claim 12 wherein said glass composite has a sealing temperature from above 400.degree. to about 450.degree. C.
14. The laminate of claim 11 including said uncoated particulate additive being selected from the group consisting of calcium fluoride and barium fluoride.
15. The laminate of claim 1 wherein about 0.1 to about 2 wt. % of said copper oxide is dissolved into said glass matrix.
16. The laminate of claim 15 wherein about 1.4 wt. % of said copper oxide is dissolved into said glass matrix.
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| 4185139 | January 22, 1980 | Smernos |
| 4405722 | September 20, 1983 | Kokubu et al. |
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| 4532222 | July 30, 1985 | Butt |
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Type: Grant
Filed: Apr 7, 1986
Date of Patent: Jun 21, 1988
Assignee: Olin Corporation (New Haven, CT)
Inventors: Edward F. Smith, III (Madison, CT), Lewis C. Hoffman (Singer Island, FL)
Primary Examiner: John E. Kittle
Assistant Examiner: P. R. Schwartz
Attorneys: Gregory S. Rosenblatt, Paul Weinstein
Application Number: 6/848,600
International Classification: B32B 1504;
